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Merck

11772457001

Roche

TUNEL AP

sufficient for 70 tests, solution, pkg of 3.5 mL

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About This Item

UNSPSC-Code:
41105600

Form

solution

Verwendung

sufficient for 70 tests

Verpackung

pkg of 3.5 mL

Hersteller/Markenname

Roche

Versandbedingung

wet ice

Lagertemp.

2-8°C

Allgemeine Beschreibung

TUNEL AP is an alkaline phosphatase-labeled antibody used for the in situ detection of apoptosis (programmed cell death) with the TUNEL reaction followed by transmission light microscopy.
The tailing reaction using TdT, also named ISEL (in situ end labeling) or TUNEL (TdT-mediated dUTP nick end labeling), has several advantages in comparison to the in situ nick translation (ISNT) using DNA polymerase:
  • Label intensity of apoptotic cells is higher with TUNEL compared to ISNT, resulting in an increased sensitivity.
  • Kinetics of nucleotide incorporation is very rapid with TUNEL compared to the ISNT.
  • TUNEL preferentially labels apoptotic cells compared to necrotic cells.

Anwendung

TUNEL AP is an antibody that is used to convert fluorescence-based TUNEL assays into colorimetric assays suited for light microscopy. The conversion is performed by binding of an anti-fluorescein antibody to FITC-dUTP. The antibody is labeled with alkaline phosphatase (AP). The AP is visualized with a precipitating substrate, such as Fast Red or NBT/BCIP.

Komponenten

Anti-fluorescein antibody, Fab fragment from sheep, conjugated with alkaline phosphatase (AP). Ready-to-use solution.

Sonstige Hinweise

For life science research only. Not for use in diagnostic procedures.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Skin Sens. 1

Lagerklassenschlüssel

12 - Non Combustible Liquids

WGK

WGK 1

Flammpunkt (°F)

No data available

Flammpunkt (°C)

No data available


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R Gold et al.
The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society, 41(7), 1023-1030 (1993-07-01)
Since DNA fragmentation is a key feature of programmed cell death (PCD) and also occurs in certain stages of necrosis, we have adapted the methodology of in situ nick-translation (ISNT) to detect DNA fragmentation on a single-cell level. We first
Beina Chen et al.
Communications biology, 5(1), 105-105 (2022-02-05)
Stroke causes degeneration and death of neurones leading to the loss of motor function and frequent occurrence of cognitive impairment and depression. Lithium (Li+), the archetypal mood stabiliser, is neuroprotective in animal models of stroke, albeit underlying mechanisms remain unknown.
Wu Jiang et al.
Clinical and experimental pharmacology & physiology, 49(1), 122-133 (2021-09-09)
Previous studies reveal that hydrogen sulphide (H2 S) exerts neuroprotection against neurotoxin-induced Parkinson's disease (PD), but the underlying mechanism remains elusive. The present study was aimed to investigate whether H2 S inhibits neuronal apoptosis of substantia nigra with the involvement
W Gorczyca et al.
Cytometry, 15(2), 169-175 (1994-02-01)
The predominant mode of either spontaneous or drug-induced death of cells in tumors is apoptosis. A flow cytometric method was developed in our laboratory to identify apoptotic cells, based on labeling DNA strand breaks, which appear as a result of
Simultaneous determination of cell surface antigens and apoptosis.
R Sgonc et al.
Trends in genetics : TIG, 10(2), 41-42 (1994-02-01)

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